Imaging normal and abnormal brain development: new perspectives for child psychiatry

References

• Rutter M, Graham P, Yule W. A neuropsychiatric study in Childhood. Clinics in Developmental Medicine. S.I.M.P./Heinemann, London 1970, Nos 35, 36
   Google Scholar
• Goodman R. Brain disorders. Child and adolescent psychiatry: modern approaches3rd edn., M Rutter, E Taylor, L Hersov. Blackwell, London 1994; 172–190
   Google Scholar
• Jernigan T L, Tallal P. Late childhood changes in brain morphology observable with MRI. Developmental Medicine and Child Neurology 1990; 32: 379–385
   PubMed Web of Science ®Google Scholar
• Reiss A L, Abrams M T, Singer H S, Ross J L, Denckla M B. Brain development, gender and IQ in children. A volumetric imaging study. Brain 1996; 1119: 1763–1774
   Web of Science ®Google Scholar
• Giedd J, Snell J, Lange N, et al. Quantitative magnetic resonance imaging of human brain development ages 4–18. Cerebral Cortex 1996; 6: 551–560
   PubMed Web of Science ®Google Scholar
• Sowell E R, Thompson P M, Holmes C J, Jernigan T, Toga A W. In vivo evidence for post-adolescent brain maturation in frontal and striatal regions. Nature Neuroscience 1999; 2: 859–861
   PubMed Web of Science ®Google Scholar
• Sowell E R, Thompson P M, Holmes C J, Batth R, Jernigan T L, Toga A W. Localizing age-related changes in brain structure between childhood and adolescence using statistical parametric mapping. Neuroimage 1999; 9: 587–597
   PubMed Web of Science ®Google Scholar
• Giedd J N, Blumenthal J, Jeffries N O, et al. Cerebral cortical gray matter changes during childhood and adolescence: a longitudinal MRI study. Nature Neuroscience 1999; 2: 861–863
   PubMed Web of Science ®Google Scholar
• Paus T, Zijdenbos A, Worsley K, et al. Structural maturation of neural pathways in children and adolescents: in vivo study. Science 1999; 283: 1908–1911
   PubMed Web of Science ®Google Scholar
• Schapiro M, Luxenberg J, Kay J, Haxby J, Friedland R, Rapoport S I. Serial quantitative estimates of brain morphmetrics in Downs syndrome at different ages. Neurology 1989; 39: 1349–1353
   PubMed Web of Science ®Google Scholar
• Reiss A, Eliez S, Schmitt J E, Patwardhan A, Haberecht M. Brain imaging in neurogenic conditions: realizing the potential of behavioural neurogenetics research. Mental Retardation and Developmental Disabilities Research Reviews 2000; 6: 186–197
   PubMedGoogle Scholar
• Aylward E H, Reiss A L, Reader M J, Singer H S, Brown J E, Denckla M B. Basal ganglia volumes in children with attention-deficit hyperactivity disorder. Journal of Child Neurology 1996; 11: 112–115
   PubMed Web of Science ®Google Scholar
• Filipek P A, Semrud-Clikeman M, Steingard R J, Renshaw P F, Kennedy D N, Biederman J. Volumetric MRI analysis comparing attention-deficit hyperactivity disorder with normal controls. Neurology 1997; 48: 589–601
   PubMed Web of Science ®Google Scholar
• Bullmore E T, Suckling J, Overmeyer S, Rabe-Hesketh S, Taylor E, Brammer M J. Global, voxel, and cluster tests, by theory and permutation, for a difference between two groups of structural MR images of the brain. IEEE Transactions of Medical Imaging 1999; 18: 32–42
   PubMed Web of Science ®Google Scholar
• Castellanos F X, Giedd J N, Marsh W L, et al. Quantitative brain magnetic resonance imaging in attention-deficit hyperactivity disorder. Archives of General Psychiatry 1996; 53: 607–616
   PubMed Web of Science ®Google Scholar
• Castellanos F X, Giedd J N, Berquin P C, et al. Quantitative brain magnetic resonance imaging in girls with attention-deficit/ hyperactivity disorder. Archives of General Psychiatry, 2001; 58: 289–295
   PubMed Web of Science ®Google Scholar
• Mataró M, García-Sánchez C, Junqué C, Estévez-González A, Pujol J. Magnetic resonance imaging measurement of the caudate nucleus in adolescents with attention-deficit hyperactivity disorder and its relationship with neuropsychological and behavioral measures. Archives of Neurology 1997; 54: 963–968
   PubMed Web of Science ®Google Scholar
• Berquin P C, Giedd J N, Jacobsen L K, et al. Cerebellum in attention-deficit hyperactivity disorder: a morphometric MRI study. Neurology 1998; 50: 1087–1093
   PubMed Web of Science ®Google Scholar
• Mostofsky S H, Reiss A L, Lockhart P, Denckla M B. Evaluation of cerebellar size in attention-deficit hyperactivity disorder. Journal of Child Neurology 1998; 13: 434–439
   PubMed Web of Science ®Google Scholar
• Castellanos F X, Swanson J. Biological underpinnings of ADHD. Hyperactivity and attention disorders of children, S Sandberg. Cambridge University Press, Cambridge UK in press
   Google Scholar
• Castellanos F X, Giedd J, Walter J, et al. Longitudinal MRI in attention-deficit/hyperactivity disorder (ADHD): effects of prior stimulant treatment in cerebellum and total brain [Abstract]. Society for Neuroscience Abstracts 2000; 26: 1327
   Google Scholar
• Nicolson R, Rapoport J. Childhood onset schizophrenia: rare but worth studying. Biological Psychiatry 1999; 46: 1418–1428
   PubMed Web of Science ®Google Scholar
• Frazier J A, Giedd J N, Hamburger S D, et al. Brain anatomic magnetic resonance imaging in childhood-onset schizophrenia. Archives of General Psychiatry 1996; 53: 617–624
   PubMed Web of Science ®Google Scholar
• Kumra S, Giedd J N, Vaituzis A C, et al. Childhood-onset psychotic disorders: quantitative magnetic resonance imaging of structural brain abnormalities. American Journal of Psychiatry 2000; 157: 1464–1474
   Web of Science ®Google Scholar
• Jacobsen L K, Giedd J N, Castellanos F X, et al. Progressive reduction of temporal lobe structures in childhood onset schizophrenia. American Journal of Psychiatry 1998; 155: 678–685
   PubMed Web of Science ®Google Scholar
• Rapoport J L, Giedd J, Kumra S, et al. Childhood-onset schizophrenia: progressive ventricular change during adolescence. Archives of General Psychiatry 1997; 54: 897–903
   PubMed Web of Science ®Google Scholar
• Giedd J N, Jeffries N O, Blumenthal J, et al. Childhood onset schizophrenia. Progressive brain changes during adolescence. Journal of Biological Psychiatry 1999; 46: 892–898
   PubMed Web of Science ®Google Scholar
• Rapoport J L, Giedd J N, Blumenthal J, et al. Progressive cortical change during adolescence in childhood-onset schizophrenia: a longitudinal magnetic resonance imaging study. Archives of General Psychiatry 1999; 56: 649–654
   PubMed Web of Science ®Google Scholar
• Bedwell J, Keller B, Smith A, Hamburger S, Kumra S, Rapoport J L. Childhood onset schizophrenia: post-psychotic decline in IQ. American Journal of Psychiatry 1999; 156: 1996–1997
   PubMed Web of Science ®Google Scholar
• Karp B I, Garvey M, Jacobsen L K, et al. Abnormal neurological maturation in early-onset schizophrenia. American Journal of Psychiatry 2001; 158: 118–122
   PubMed Web of Science ®Google Scholar
• Nicolson R, Lenane M, Brookner F, et al. Children and adolescents with psychotic disorder not otherwise specified: a two to eight year follow-up. Comprehensive Psychiatry in press
   Google Scholar
• Nicolson R, Giedd J N, Blumenthal J, et al. Lack of progressive cortical gray matter with non-schizophrenic psychotic disorders. Biological Psychiatry in press
   Google Scholar
• Glantz L, Lewis D. Decreased dendritic spine density on prefrontal cortical pyramidal neurons in schizophrenia. Archives of General Psychiatry 2000; 57: 65–73
   PubMed Web of Science ®Google Scholar
• Selemon L, Goldman-Rakic P. The reduced neuropil hypothesis: a circuit based model of schizophrenia. Biological Psychiatry 1999; 45: 17–25
   PubMed Web of Science ®Google Scholar
• McGlashan T H, Hoffman R E. Schizophrenia as a disorder of developmentally reduced synaptic connectivity. Archives of General Psychiatry 2000; 57: 637–648
   PubMed Web of Science ®Google Scholar
• Woods B T. Is schizophrenia a progressive neurodevelopmental disorder? Toward a unitary pathogenetic mechanism. American Journal of Psychiatry 1998; 155: 161–170
   Web of Science ®Google Scholar
• Keshavan M S, Hogarty G E. Brain maturational processes and delayed onset in schizophrenia. Development and Psychopathology 1999; 11: 525–543
   PubMed Web of Science ®Google Scholar
• Allen R W, Young S L. Phencyclidine-induced psychosis. American Journal of Psychiatry 1978; 135: 1081–1084
   PubMed Web of Science ®Google Scholar
• Friston K J. Schizophrenia and the disconnection hypothesis. Acta Psychiatrica Scandinavica 1999; 99: 68–79
   PubMed Web of Science ®Google Scholar
• Benes F M, Davidson J, Bird E D. Quantitative cytoarchitectural studies of the cerebral cortex of schizophrenics. Archives of General Psychiatry 1986; 43: 31–35
   PubMed Web of Science ®Google Scholar
• Hubel D H, Wiesel T N, LeVay S. Plasticity of ocular dominance columns in monkey striate cortex. Philosophical Transactions of the Royal Society of London, Series B. Biological Sciences 1977; 278: 377–409
   PubMed Web of Science ®Google Scholar
• Singer W. Neuronal mechanisms in experience dependent modification of visual cortex function. Progress in Brain Research 1979; 51: 457–477
   PubMedGoogle Scholar
• Greenough W, Black J. Induction of brain structure by experience: substrate for cognitive development. Minnesota symposia on child psychology 24: developmental behavioral neuroscience, M R Gunnar, C A Nelson. Lawrence Erlbaum, Hillandale, NJ 1991; 155–200
   Google Scholar
• Haracz J L. Neural plasticity in schizophrenia. Schizophrenia Bulletin 1985; 11: 191–240
   PubMed Web of Science ®Google Scholar
• Rutledge L T. Effects of cortical denervation and stimulation on axon, dendrites, and synapses. Neural plasticity, C W Cotman. Raven, New York 1978; 273–289
   Google Scholar
• Chen S, Hillman D E. Plasticity of the parallel fiber-Purkinje cell synapse by spine takeover and new synapse formation in the adult rat. Brain Research 1982; 240: 205–220
   PubMed Web of Science ®Google Scholar
• Volpe J J. Overview: normal and abnormal human brain development. Mental Retardation and Developmental Disabilities Research Reviews 2000; 6: 1–5
   PubMedGoogle Scholar
• Evrard P, Marret S, Gressens P. Environmental and genetic determinants of neural migration and postmigratory survival. Acta Paediatrica 1997; 422(Suppl.)20–26
   Google Scholar
• Riddle D R, McAllister A K, Lo D C, Katz L C. Neurotrophins in cortical development. Cold Spring Harbor symposium on Quantitative Biology. 1996; 61: 85–93
   Google Scholar
• Johnston M V. Neurotransmitters and vulnerability of the developing brain. Brain and Development 1995; 17: 301–306
   PubMed Web of Science ®Google Scholar
• Milberger S, Biederman J, Faraone S V, Guite J, Tsuang M T. Pregnancy, delivery and infancy complications and attention deficit hyperactivity disorder: issues of gene–environment interaction. Biological Psychiatry 1997; 41: 65–75
   PubMed Web of Science ®Google Scholar
• Melchitzky D S, Lewis D A. Tyrosine hydroxylase- and dopamine transporter-immunoreactive axons in the primate cerebellum. Evidence for a lobular- and laminar-specific dopamine innervation. Neuropsychopharmacology 2000; 22: 466–472
   PubMed Web of Science ®Google Scholar
• Seroogy K B, Lundgren K H, Tran T M, Guthrie K M, Isackson P J, Gall C M. Dopaminergic neurons in rat ventral midbrain express brain-derived neurotrophic factor and neurotrophin-3 mRNAs. Journal of Comparative Neurology 1994; 342: 321–334
   PubMed Web of Science ®Google Scholar
• Castellanos F X. Toward a pathophysiology of attention-deficit/ hyperactivity disorder. Clinical Pediatrics 1997; 36: 381–393
   PubMed Web of Science ®Google Scholar
• Castellanos F X, Lau E, Tayebi N, et al. Lack of an association between dopamine-4 receptor polymorphism and attention-deficit/hyperactivity disorder: genetic and brain morphometric analyses. Molecular Biology 1998; 3: 431–434
   Google Scholar
• Castellanos F X, Giedd J N, Eckburg P, et al. Quantitative morphology of the caudate nucleus in attention deficit hyperactivity disorder. American Journal of Psychiatry 1994; 151: 1791–1796
   PubMed Web of Science ®Google Scholar
• Hynd G W, Hern K L, Novey E S, et al. Attention deficit-hyperactivity disorder and asymmetry of the caudate nucleus. Journal of Child Neurology 1993; 8: 339–347
   PubMed Web of Science ®Google Scholar
• Sawada H, Shimohama S. Neuroprotective effects of estradiol in mesencephalic dopaminergic neurons. Neuroscience and Biobehavioral Reviews 2000; 24: 143–147
   PubMed Web of Science ®Google Scholar
• Arnold S. Neurodevelopmental abnormalities in schizophrenia: insights from neuropathology. Development and Psychopathology 1999; 11: 439–456
   PubMed Web of Science ®Google Scholar
• Harrison P. The neuropathology of schizophrenia: a critical review of the data and their interpretation. Brain 1999; 122: 593–624
   PubMed Web of Science ®Google Scholar
• Huttenlocher P R, Dabholkar A S. Regional differences in synaptogenesis in human cerebral cortex. Journal of Comparative Neurology 1997; 387: 167–178
   PubMed Web of Science ®Google Scholar
• Selemon L D, Rajkowska G, Goldman-Rakic P S. Abnormally high neuronal density in the schizophrenic cortex: a morphometric analysis of the prefrontal area 9 and occipital area 17. Archives of General Psychiatry 1995; 52: 805–818
   PubMed Web of Science ®Google Scholar
• Selemon L D, Rajkowska G, Goldman-Rakic P S. Elevated neuronal density in prefrontal area 46 in brains from schizophrenic patients: application of a three-dimensional stereologic method. Journal of Comparative Neurology 1998; 392: 402–412
   PubMed Web of Science ®Google Scholar
• Pakkenberg R. Total nerve cell number in neocortex in chronic schizophrenics and controls estimated using optical dissectors. Biological Psychiatry 1993; 34: 768–772
   PubMed Web of Science ®Google Scholar
• Glantz L A, Lewis D A. Reduction of synaptophysin immunoreactivity in the prefrontal cortex or schizophrenic subjects: regional and diagnostic specificity. Archives of General Psychiatry 1997; 54: 660–669
   PubMed Web of Science ®Google Scholar
• Mirnics K, Middleton F, Murquez A, Lewis D A, Levitt P. Molecular characterization of schizophrenia viewed by microarray analysis of gene expression in prefrontal cortex. Neuron 2000; 28: 53–67
   PubMed Web of Science ®Google Scholar
• Lohof A M, Delhaye-Bouchaud N, Mariani J. Synapse elimination in the central nervous system: functional significance and cellular mechanisms. Reviews in the Neurosciences 1996; 7: 85–101
   PubMed Web of Science ®Google Scholar
• Thompson W J. Activity and synapse elimination at the neuromuscular junction. Cellular and Molecular Neurobiology 1985; 5: 167–182
   PubMed Web of Science ®Google Scholar
• Lanuza M A, Li M, Jia M, et al. Protein kinase C-mediated changes in synaptic efficacy at the neuromuscular junction in vitro: the role of postsynaptic acetylcholinereceptors. Journal of Neuroscience Research 2000; 61: 616–625
   PubMed Web of Science ®Google Scholar
• Balice-Gordon R J, Lichtman J W. Long-term synapse loss induced by focal blockade of postsynaptic receptors. Nature 1994; 372: 519–524
   PubMed Web of Science ®Google Scholar
• Kano M, Hashimato K, Chen C, et al. Impaired synapse elimination during cerebellar development in PKCγ mutant mice. Cell 1995; 83: 1223–1231
   PubMed Web of Science ®Google Scholar
• Hughes R A, Sendtner M, Thoenen H. Members of several gene families influence survival of rat motor neurons in vitro and in vivo. Journal of Neuroscience Research 1993; 36: 663–671
   PubMed Web of Science ®Google Scholar
• Thoenen H. Neurotrophins and neuronal plasticity. Science 1995; 270: 593–598
   PubMed Web of Science ®Google Scholar
• McAllister A K, Katz L, Lo D. Neurotrophins and synaptic plasticity. Annual Review of Neuroscience 1999; 22: 295–318
   PubMed Web of Science ®Google Scholar
• Cabelli R J, Shelton D L, Segal D L, Shatz C. Blockage of endogenous ligand of trI: B inhibits formation of endogenous ocular dominance columns. Neuron 1997; 19: 63–76
   PubMed Web of Science ®Google Scholar
• Feinberg I. Schizophrenia: caused by a fault in programmed synaptic elimination during adolescence?. Journal of Psychiatric Research 1982/1983; 17: 319–334
   PubMed Web of Science ®Google Scholar
• Semrud-Clikeman M, Steingard R J, Filipek P, et al. Using MRI to examine brain-behaviour relationships in males with attention deficit hyperactivity. Journal of the American Academy of Child and Adolescent Psychiatry 2000; 39: 477–484
   PubMed Web of Science ®Google Scholar
• Mataro M, Garcia-Sanchez C, Junque C, Estevez-Gonzalez A, Pujol J. Magnetic resonance imaging measurement of the caudate nucleus in adolescents with attention-deficit hyperactivity disorder and its relationship with neuropsychological and behavioural measures. Archives of Neurobiology 1997; 54: 963–968
   PubMed Web of Science ®Google Scholar